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You will support the design, writing and operational documentation of multi-country investigator-initiated trials and translational oncology studies under the ATORG platform. This includes drafting study protocols, scientific reports and stakeholder materials, and contributing to consensus meetings and academic outputs. You will coordinate protocol input from principal investigators, statisticians, clinicians and vendors, and adapt study designs to site capabilities and scientific objectives. You will also prepare abstracts, posters, manuscripts, grant applications and meeting materials, and liaise with site investigators, pharma sponsors, CROs and academic partners.
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